Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
15 | g.73324120C>A | CA393089924 | HCN4 | c.2112G>T (p.Glu704Asp) c.894G>T (p.Glu298Asp) | |
15 | g.73324120C= | CA2187189064 | HCN4 | c.2112G= (p.Glu704=) c.894G= (p.Glu298=) | |
15 | g.73324120C>G | CA393089926 | HCN4 | c.2112G>C (p.Glu704Asp) c.894G>C (p.Glu298Asp) | |
15 | g.73324120C>T | CA7649126 | HCN4 | c.2112G>A (p.Glu704=) c.894G>A (p.Glu298=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
15 | g.73324121T>A | CA393089929 | HCN4 | c.2111A>T (p.Glu704Val) c.893A>T (p.Glu298Val) | |
15 | g.73324121T>C | CA393089931 | HCN4 | c.2111A>G (p.Glu704Gly) c.893A>G (p.Glu298Gly) | |
15 | g.73324121T>G | CA393089933 | HCN4 | c.2111A>C (p.Glu704Ala) c.893A>C (p.Glu298Ala) | |
15 | g.73324122C>A | CA393089935 | HCN4 | c.2110G>T (p.Glu704Ter) c.892G>T (p.Glu298Ter) | |
15 | g.73324122C>G | CA393089939 | HCN4 | c.2110G>C (p.Glu704Gln) c.892G>C (p.Glu298Gln) | |
15 | g.73324122C>T | CA393089937 | HCN4 | c.2110G>A (p.Glu704Lys) c.892G>A (p.Glu298Lys) | ClinVar gnomAD v4 COSMIC |
15 | g.73324123G>A | CA7649127 | HCN4 | c.2109C>T (p.Phe703=) c.891C>T (p.Phe297=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
15 | g.73324123G>C | CA393089943 | HCN4 | c.2109C>G (p.Phe703Leu) c.891C>G (p.Phe297Leu) | |
15 | g.73324123G= | CA2187189069 | HCN4 | c.2109C= (p.Phe703=) c.891C= (p.Phe297=) | |
15 | g.73324123G>T | CA393089945 | HCN4 | c.2109C>A (p.Phe703Leu) c.891C>A (p.Phe297Leu) | |
15 | g.73324124A>C | CA393089947 | HCN4 | c.2108T>G (p.Phe703Cys) c.890T>G (p.Phe297Cys) | |
15 | g.73324124A>G | CA393089949 | HCN4 | c.2108T>C (p.Phe703Ser) c.890T>C (p.Phe297Ser) | |
15 | g.73324124A>T | CA393089950 | HCN4 | c.2108T>A (p.Phe703Tyr) c.890T>A (p.Phe297Tyr) | |
15 | g.73324125A>C | CA393089953 | HCN4 | c.2107T>G (p.Phe703Val) c.889T>G (p.Phe297Val) | |
15 | g.73324125A>G | CA393089956 | HCN4 | c.2107T>C (p.Phe703Leu) c.889T>C (p.Phe297Leu) | ClinVar |
15 | g.73324125A>T | CA393089958 | HCN4 | c.2107T>A (p.Phe703Ile) c.889T>A (p.Phe297Ile) | |
15 | g.73324126G>A | CA272665439 | HCN4 | c.2106C>T (p.Ala702=) c.888C>T (p.Ala296=) | dbSNP gnomAD v3 gnomAD v4 |
15 | g.73324126G>C | CA491478840 | HCN4 | c.2106C>G (p.Ala702=) c.888C>G (p.Ala296=) | |
15 | g.73324126G= | CA2187189075 | HCN4 | c.2106C= (p.Ala702=) c.888C= (p.Ala296=) | |
15 | g.73324126G>T | CA491478838 | HCN4 | c.2106C>A (p.Ala702=) c.888C>A (p.Ala296=) | |
15 | g.73324127G>A | CA393089962 | HCN4 | c.2105C>T (p.Ala702Val) c.887C>T (p.Ala296Val) | |
15 | g.73324127G>C | CA393089963 | HCN4 | c.2105C>G (p.Ala702Gly) c.887C>G (p.Ala296Gly) | |
15 | g.73324127G>T | CA393089964 | HCN4 | c.2105C>A (p.Ala702Asp) c.887C>A (p.Ala296Asp) | |
15 | g.73324128C>A | CA393089970 | HCN4 | c.2104G>T (p.Ala702Ser) c.886G>T (p.Ala296Ser) | |
15 | g.73324128C= | CA2187189077 | HCN4 | c.2104G= (p.Ala702=) c.886G= (p.Ala296=) | |
15 | g.73324128C>G | CA393089965 | HCN4 | c.2104G>C (p.Ala702Pro) c.886G>C (p.Ala296Pro) | |
15 | g.73324128C>T | CA393089967 | HCN4 | c.2104G>A (p.Ala702Thr) c.886G>A (p.Ala296Thr) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
15 | g.73324129C>A | CA393089971 | HCN4 | c.2103G>T (p.Arg701Ser) c.885G>T (p.Arg295Ser) | |
15 | g.73324129C>G | CA393089973 | HCN4 | c.2103G>C (p.Arg701Ser) c.885G>C (p.Arg295Ser) | |
15 | g.73324129C>T | CA491478847 | HCN4 | c.2103G>A (p.Arg701=) c.885G>A (p.Arg295=) | |
15 | g.73324130C>A | CA393089975 | HCN4 | c.2102G>T (p.Arg701Met) c.884G>T (p.Arg295Met) | |
15 | g.73324130C>G | CA393089976 | HCN4 | c.2102G>C (p.Arg701Thr) c.884G>C (p.Arg295Thr) | |
15 | g.73324130C>T | CA393089978 | HCN4 | c.2102G>A (p.Arg701Lys) c.884G>A (p.Arg295Lys) | |
15 | g.73324131T>A | CA393089980 | HCN4 | c.2101A>T (p.Arg701Trp) c.883A>T (p.Arg295Trp) | |
15 | g.73324131T>C | CA393089981 | HCN4 | c.2101A>G (p.Arg701Gly) c.883A>G (p.Arg295Gly) | |
15 | g.73324131T>G | CA491478851 | HCN4 | c.2101A>C (p.Arg701=) c.883A>C (p.Arg295=) | |
15 | g.73324132T>A | CA491478852 | HCN4 | c.2100A>T (p.Arg700=) c.882A>T (p.Arg294=) | |
15 | g.73324132T>C | CA491478853 | HCN4 | c.2100A>G (p.Arg700=) c.882A>G (p.Arg294=) | |
15 | g.73324132T>G | CA491478854 | HCN4 | c.2100A>C (p.Arg700=) c.882A>C (p.Arg294=) | |
15 | g.73324133C>A | CA393089983 | HCN4 | c.2099G>T (p.Arg700Leu) c.881G>T (p.Arg294Leu) | |
15 | g.73324133C= | CA2187189079 | HCN4 | c.2099G= (p.Arg700=) c.881G= (p.Arg294=) | |
15 | g.73324133C>G | CA393089985 | HCN4 | c.2099G>C (p.Arg700Pro) c.881G>C (p.Arg294Pro) | |
15 | g.73324133C>T | CA393089987 | HCN4 | c.2099G>A (p.Arg700Gln) c.881G>A (p.Arg294Gln) | ClinVar dbSNP COSMIC |
15 | g.73324134G>A | CA393089989 | HCN4 | c.2098C>T (p.Arg700Ter) c.880C>T (p.Arg294Ter) | gnomAD v4 COSMIC |
15 | g.73324134G>C | CA393089990 | HCN4 | c.2098C>G (p.Arg700Gly) c.880C>G (p.Arg294Gly) | |
15 | g.73324134G>T | CA491478858 | HCN4 | c.2098C>A (p.Arg700=) c.880C>A (p.Arg294=) |